Maternal Collapse in Pregnancy and the Puerperium

Key Points

  • Maternal collapse is a rare but life-threatening event, with a wide-ranging aetiology. The outcome primarily for the mother, but also for the fetus, depends on prompt and effective resuscitation.

  • An obstetric modified early warning score chart along with clinical judgment should be used for all women undergoing observation to allow for early recognition of the woman who is becoming critically ill.

  • Consider 4 ‘H’s and 4 ‘T’s for the cause of the maternal cardiac arrest; in the pregnant woman, add eclampsia and intracranial haemorrhage.

  • Maternal collapse resuscitation should follow the Resuscitation Council (UK) 2021 guidelines (Appendix 1) using the standard ABCDE approach, with some modifications for maternal physiology, in particular relief of aortocaval compression.

  • If maternal cardiac arrest occurs in the community setting, 999 call should be made, basic life support should be administered, and rapid transfer arranged.

  • Senior staff with appropriate experience should be involved at an early stage.

  • Perimortem Caesarean Section (PMCS) should be seen as a resuscitative procedure to be performed primarily in the interests of maternal survival.

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Abbreviations

AFEAmniotic Fluid Embolism
CPRCardioPulmonary Resuscitation
MEOWSModified Early Obstetric Warning System

Introduction

Maternal collapse is defined as an acute event involving the cardiorespiratory systems and/or central nervous system resulting in a reduced or absent conscious level (and potentially cardiac arrest and death), at any stage in pregnancy and up to 6 weeks after birth1.

The incidence of cardiac arrest in pregnancy is much rarer than maternal collapse at around 1: 36,000 maternities, with a case fatality rate of 42%. Causes of maternal cardiac arrest vary including hypovolaemia, thromboembolic disease, amniotic fluid embolism and cardiac causes with a significant mortality rate if occurring in the community. 25% of collapses were attributed to obstetric anaesthesia, all of whom were successfully resuscitated2.

An obstetric modified early warning score chart along with clinical judgment should be used to allow early recognition of the woman who is becoming critically ill1. For full guideline, see Recognising Deterioration in Pregnant or Recently Delivered Women and Use of Modified Obstetric Warning System (MEOWS).

It is essential that the clinical team are skilled in initial effective resuscitation techniques and are able to investigate and diagnose the cause of the collapse to allow appropriate, directed ongoing management 3,4.

Early involvement of senior experienced staff, including obstetricians, anaesthetists, haematologists and intensivists, is essential to optimise outcome.

2. Causes of Maternal Collapse

2.1 General

Maternal collapse can result from many causes which may or may not be pregnancy related.

A systematic approach to assessment facilitates identification of the cause of collapse. If the cause is reversible, the survival rates are greater and those for which specific treatment exists must be rapidly considered 5.

A systematic ABCDE approach should enable the clinical team to identify the most common causes of cardiac arrest. Consider 4 ‘H’s and 4 ‘T’s and, in the pregnant woman, add eclampsia and intracranial haemorrhage.

4 Hs

Reversible causeCause in pregnancy
HypovolaemiaBleeding (obstetric/other; may be concealed) or relative hypovolaemia due to dense spinal block, septic or neurogenic shock and anaphylaxis
HypoxiaPregnant women can become hypoxic more quickly.
Cardiac events – peripartum cardiomyopathy, myocardial infarction, aortic dissection, large vessel aneurysms
Hypo/hyperkalaemiaNo more likely; severe hyperemesis
Hypo/hypernatraemiaMay be caused by oxytocin use
Iatrogenic administration of fluids in labour/ women’s desire to “drink plenty of fluid” in labour
HypothermiaNo more likely
Reversible causeCause in pregnancy

4 Ts

Reversible causeCause in pregnancy
ThromboembolismAmniotic fluid embolism, pulmonary embolus, air embolus, Myocardial infarction
ToxicityLocal anaesthetic, magnesium, other
Tension pneumothoraxFollowing trauma/suicide attempts
TamponadeFollowing trauma/suicide attempts

Eclampsia and pre-eclampsia

Intracranial Haemorrhage

[Resuscitation Council (UK) 2021.]

2.2 Haemorrhage

Major obstetric haemorrhage was responsible for 17 maternal deaths between 2019-2021 with an estimated incidence of 8 in 1000 maternities6. Cause of major obstetric haemorrhage include postpartum haemorrhage, major antepartum haemorrhage from placenta praevia, placental abruption, uterine rupture and ectopic pregnancy. Concealed haemorrhage should not be forgotten including following Caesarian section and ruptured ectopic pregnancy. Blood loss is often difficult to estimate and fit healthy women can tolerate significant loss prior to showing signs of decompensation1. For full guidance, refer to the Antepartum haemorrhage guideline.

In the case of maternal collapse secondary to antepartum haemorrhage, the fetus and placenta should be delivered promptly to allow control of the haemorrhage.

In the case of massive placental abruption, Caesarean section may occasionally be indicated even if the fetus is dead to allow rapid control of the haemorrhage.

Intravenous tranexamic acid significantly reduces mortality due to postpartum haemorrhage.

Point of Care ROTEM Machine should be used along with the other laboratory tests that are requested in the whole blood at the time of PPH. Its viscoelasticity technology would detect coagulation status (Platelets, Fibrinogen and Coagulation factors) and provide an overview of patient's whole blood sample in 10 minutes.

2.3 Thromboembolism

Thromboembolism is the leading cause of direct maternal death during or up to 6 weeks after the end of the pregnancy leading to the deaths of 33 women in the MBRRACE report 2019-2021.

For full guidance, refer to Thromboprophylaxis and the treatment of venous thromboembolism in pregnancy and the puerperium.

2.4 Cardiac disease

Cardiac disease remains the commonest cause of indirect maternal death and the commonest cause of maternal death overall when excluding maternal deaths from Covid-19. Between 2019 and 2021, there were 33 women that died from cardiac causes in the UK during pregnancy or within 42 days of delivery6.

The majority of deaths secondary to cardiac causes occur in women with no previous history. The main cardiac causes of maternal death are ischaemia and sudden arrhythmic cardiac death with a structurally normal heart. Aortic root dissection, although usually associated with an inherited aortopathy can present in otherwise healthy women, and signs and symptoms, such as central chest or interscapular pain, a wide pulse pressure (mainly secondary to systolic hypertension) and a new cardiac murmur, must prompt appropriate imaging and, if required, referral to a cardiologist. The incidence of congenital and rheumatic heart disease in pregnancy is increasing, secondary to increased survival rates and with improved management of congenital heart disease. In addition, women with mechanical prosthetic heart valves are at particularly increased risk of complications in pregnancy. Other cardiac causes include cardiomyopathy; dissection of the coronary artery; acute left ventricular failure; infective endocarditis; and pulmonary oedema.

After successful resuscitation, cardiac cases should be managed by an expert cardiology team.

2.5 Sepsis

Sepsis is a significant cause of maternal morbidity and mortality. Bacteraemia which can be present in the absence of pyrexia or a raised white cell count, can progress rapidly to severe sepsis and septic shock leading to collapse1.

Septic shock should be managed in accordance with the Surviving Sepsis Campaign guidelines.

For full guidance refer to the Management of sepsis in pregnancy and puerperium guideline.

2.6 Amniotic fluid Embolism

UK Incidence of Amniotic Fluid Embolism (AFE) reported in the 2019-2021 MBRRACE report was 0.39 per 100,000 maternities. AFE presents as a collapse during labour or birth, or within (usually) 30 minutes of birth in the form of hypotension, respiratory distress and acute hypoxia. Seizures and cardiac arrest may also occur1. This is followed by acute coagulopathy in those women who survive the initial event. AFE incidence is increased in women who have multiple pregnancy, polyhydramnios, placenta praevia, placental abruption and induction of labour7. If AFE is suspected or proved, the UK National Registry for AFE should be contacted.

The management of AFE is supportive rather than specific, as there is no proven effective therapy.

Point of Care ROTEM Machine should be used along with the other laboratory tests that are requested in the whole blood at the time of the event. Its viscoelasticity technology would detect coagulation status (Platelets, Fibrinogen and Coagulation factors) and provide an overview of patient's whole blood sample in 10 minutes.

Coagulopathy needs early, aggressive treatment, including the use of fresh frozen plasma.

Recombinant factor VII should only be used if coagulopathy cannot be corrected by massive blood component replacement as it has been associated with poorer outcome in women with AFE**.**

2.7 Drug toxicity and overdose

Drug toxicity and overdose should be considered in all cases of collapse. Substance misuse should be remembered as a potential cause of collapse, especially outside of hospital.

Therapeutic drug toxicity is possible with commonly used drugs in obstetric practice such as magnesium sulphate in the presence of renal impairment and local anaesthetic agents. The antidote to cardiac dysrhythmias, respiratory depression or resistant hypotension caused by magnesium toxicity is 6.8mmol of 10% calcium gluconate (30ml if weight >50kg) or 10% 6.8mmol 10% calcium chloride (10ml if weight > 50kg) given by slow intravenous injection over 5-10minutes. For full information, please refer to Toxbase®.

Signs and symptoms of Local Anaesthetic Toxicity

MildSevere
Tingling, numbness of the tongue or around the mouthSudden loss of consciousness
Metallic tasteTonic-clonic convulsions
Mild visual disturbancesCardiovascular collapse
Light headednessSinus bradycardia
Conduction blocks
Asystole and ventricular tachyarrhythmias

If local anaesthetic toxicity is suspected, stop injecting immediately.

Lipid rescue should be used in cases of collapse secondary to local anaesthetic toxicity.

Intralipid 20% is available on the Resuscitation trolley.

Manage arrhythmias as usual, recognising that they may be very refractory to treatment.

All cases of lipid rescue should be reported to NHS Improvement and the Lipid Rescue site.

Refer to the guideline for Management of severe local anaesthetic toxicity (Royal College of Anaesthetists).

2.8 Eclampsia

Fitting (Seizures) after 20 weeks gestation may be attributed to eclampsia, notably where there is no known history of epilepsy. However, epilepsy should always be considered in cases of maternal collapse associated with seizure activity.

For full guidance refer to the Hypertensive disorders in pregnancy guideline.

2.9 Intracranial haemorrhage

Intracranial haemorrhage is a potential complication of uncontrolled, particularly systolic hypertension, but can also result from ruptured aneurysms and arteriovenous malformations. The initial presentation may be maternal collapse, but often severe headache precedes this. Neuroradiologists and neurosurgeons should be involved in the care of pregnant women with intracranial haemorrhage at the earliest opportunity.

2.10 Anaphylaxis

Anaphylaxis is a severe, life threatening systemic hypersensitivity reaction, resulting in respiratory, cutaneous and circulatory changes, and collapse. There is significant intravascular volume redistribution, which can lead to decreased cardiac output. Acute ventricular failure and myocardial ischaemia may occur.

Airway obstruction secondary to angioedema, bronchospasm and mucous plugging of smaller airways all contributing to significant hypoxia and difficulties with ventilation1.

In cases of anaphylaxis, all potential causative agents should be removed, and the ABCDE approach to assessment and resuscitation followed.

If a cardiac arrest secondary to an anaphylactic reaction occurs in the community, the woman should have basic life support, including IM adrenaline if available, and be transferred to a hospital setting as quickly as possible, unless a suitably trained healthcare professional is present with appropriate equipment and drugs in which case definitive resuscitation and treatment should be commenced.

The treatment for anaphylaxis is 1:1000 (1mg/ml) adrenaline injection: Give 500 micrograms (0.5 ml) intramuscularly. This dose is for intramuscular use only.

3.0 Physiological and anatomical changes in pregnancy that affect resuscitation.

It is essential that anyone involved in the resuscitation of pregnant women is aware of the physiological differences.

Aortocaval compression significantly reduces cardiac output from 20 weeks of gestation onwards and the efficacy of chest compressions during resuscitation.

Changes in lung function, diaphragmatic splinting and increased oxygen consumption make pregnant women become hypoxic more readily and make ventilation more difficult.

Difficult intubation is more likely in pregnancy. Weight gain in pregnancy, large breasts inhibiting the working space and laryngeal oedema can all contribute to making intubation more difficult.

Pregnant women are also at an increased risk of aspiration.

4.0 Management of the collapsed woman

Maternal collapse resuscitation should follow the Resuscitation Council (UK) 2021 guidelines using the standard ABCDE approach, with some modifications for maternal physiology, in particular relief of aortocaval compression.

4.1 In the event of maternal collapse

  • Ensure safe to approach

  • Stimulate and assess response

  • If she responds

    • Call for help 2222 Obstetric Emergency call,
    • Place in left lateral position if tilted in theatres or, if outside this environment, manually and gently displace the uterus by placing a hand below the uterus on the maternal right and pushing the uterus slightly upwards and to the to the left to relieve aortocaval compression.
    • Give high-flow oxygen to achieve Sat O2 of at least 94%
    • Commence MEOWS chart if not already in use and escalate as appropriate
    • Assess fetal wellbeing.
    • Check blood glucose level
    • Insert 16G IV cannula
    • Take bloods for:
      • full blood count
      • group and save or crossmatch 4 units dependent on perceived cause of collapse
      • urea and electrolytes
      • clotting studies
      • Arterial blood gas/venous blood gas including lactate
      • Blood cultures should be obtained by separate venous stab as per trust guidelines.

All sample should be processed as URGENT by Pathology.

Ongoing treatment will depend on the cause of the collapse.

  • If No response

    • Call 2222 for Maternal Cardiac Arrest
    • Ensure manual uterine displacement in women above 20 weeks gestation or where the uterus is palpable at or above the level of the umbilicus.

4.2 Airway

  • Open airway

    • Check for obstruction

    • Head tilt, chin lift

  • Assess for breathing for up to 10 seconds

    • Look for chest movement, listen for breath sounds, feel for air
  • Breathing normally

    • Turn into recovery position

    • Check help is on the way

    • Assess breathing, pulse, blood pressure, fetal heart rate regularly using a MEOWS chart.

  • Not breathing , start CardioPulmonary Resuscitation (CPR) as per Resuscitation Council (UK) 2021 guidelines

The airway should be managed as soon as possible by an experienced anaesthetist.

  • Persons not directly involved with the resuscitation should ensure that:

    • The security doors are open to allow emergency access to the area.
    • The cardiac arrest trolley is taken to the room.
    • The consultant obstetrician and consultant obstetric anaesthetist should be summoned at the time of the cardiopulmonary arrest call.
    • Someone is available to act as a ‘runner’.
    • Appoint a scribe.
    • The woman’s records are available.
  • Supplemental oxygen with a gas flow 10-15 lt per minute should be administered as soon as possible.

Bag and mask ventilation should be undertaken until intubation

  • When the defibrillator arrives, apply self-adhesive defibrillation pads to the woman and analyse the rhythm. These should be applied whilst chest compressions are ongoing.

4.3 Circulation

  • Assess cardiac rhythm
Shockable RhythmNon-Shockable
VF / pulseless VTAsystole and PEA
Defibrilation with
200 j/300 j/360j biphasic
360 j monophasic
CPR 30:2 for 2 minutesImmediate CPR 30:2
  • During CPR

  • Establish IO/ IV access – ideally two wide bore cannulae should be inserted as soon as possible. If peripheral venous access is not possible early consideration of intraosseous access (IO), central venous access or venous cutdown should be considered.

  • Give adrenaline as per Advanced Life support algorithm.

  • Correct reversible causes – 4 H’s, 4T’s (see above, section 2.1)

4.4 Perimortem Caesarean Section (PMCS)

  • PMCS should be seen as a resuscitative procedure to be performed primarily in the interests of maternal survival.

  • Senior staff should be involved at an early stage.

  • In women over 20 weeks of gestation, if there is no response to correctly performed CPR within 4 minutes of maternal collapse or if resuscitation is continued beyond this, then PMCS should be undertaken to assist maternal resuscitation. Ideally, this should be achieved within 5 minutes of the collapse.

  • A scalpel and umbilical cord clamps should be available on the resuscitation trolley in all areas where maternal collapse may occur, including accident and emergency department.

  • Perimortem caesarean section should be performed where the resuscitation is taking place.

  • The operator should use the incision which will facilitate the most rapid access. This may be a midline vertical incision or a suprapubic transverse incision.

  • Where the outcome is not successful, the case should be discussed with the coroner to determine whether a post-mortem is required before any medical devices such as lines and endotracheal tubes are removed, as per the Royal College of Pathologists recommendations.

5.0 What are the outcomes for the mother and the baby?

Outcomes for mothers and babies depend on the cause of collapse, gestational age and access to emergency care, with survival rates being poorer if the collapse occurs out of hospital. In maternal cardiac arrest, maternal survival rates of over 50% have been reported.

6.0 Post resuscitation care

  • Ongoing management depends on the underlying cause of the collapse

  • It is essential the woman and baby is transferred to an appropriate environment such as high dependency or critical care area.

  • Accurate documentation is essential in all cases of maternal collapse and a critical incident form should be submitted whether or not resuscitation is successful.

  • All cases of maternal death must be reported to MBRRACE-UK

  • All maternity staff should have annual formal multidisciplinary training in generic life support and the management of maternal collapse.

  • Life support training improves resuscitation skills.

  • Small group multidisciplinary interactive practical training is recommended to improve the management of maternal collapse.

  • Debriefing is recommended for the woman, the family and the staff involved in the event.

7.0 References

1. Chu J, Johnston TA, Geoghegan J, on behalf of the Royal College of Obstetricians and Gynaecologists. Maternal collapse in Pregnancy and the Puerperium. BJOG 2020;127:e14-e52

2. Beckett VA, Knight M, Sharpe P. The CAPS Study: Incidence, management and outcomes of cardiac arrest in pregnancy in the UK: a prospective, descriptive study. BJOG 2017; 124:1374-81

3. Healthcare Improvement Scotland. Scottish Confidential Audit of Severe Maternal Morbidity: reducing avoidable harm. 10th Annual Report Edinburgh: HIS 2014.

4. Manning E, O’Farrell IB, Corcoran P, de Foubert P, Drummond L, McKernan J, et al. Severe Maternal Morbidity in Ireland Annual Report 2015. Cork: National Perinatal Epidemiology Centre; 2017

5. Resuscitation Council UK (2021) Adult advanced life support. https://www.resus.org.uk/library/2021-resuscitation-guidelines/adult-advanced-life-support-guidelines

6. Knight M, Bunch K, Tuffnell D, Shakespeare J, Kotnis R, Kenyon S, Kurinczuk J. Saving Lives, Improving mother’s care. Lessons learned to inform Maternity Care from the UK and Ireland Confidential Enquiries into Maternal Deaths and Morbidity 2019-2021. Oxford: National Perinatal Epidemiology Unit, University of Oxford 2023.

7. Fitzpatrick K.E., Van Den Akker T, Bloemenkamp K.W.M, Risk factors, management and outcomes of Amniotic Fluid Embolism: A Multicountry population-based cohort and nested case control study. PLOS Medicine Nov 2019

Appendix - Obstetric Cardiac Arrest (Rescuscitation Council UK 2021)

Full version control record

Version:2.0
Guidelines Leads:Miss Petya Doncheva, Consultant Obstetrician and Gynaecologist, WPH
Miss Sukhera Furness, Consultant Obstetrician and Gynaecologist, FPH
Lead Director/ Chief of Service:Miss Anne Deans, Chief of Service for Obstetrics and Gynaecology
Library check completed:13 September 2024
Professional midwifery advocates:Maria Thomsen, Angeliki Karava-Sood
Ratified at:Cross Site Obstetric Clinical Governance meeting, 16 December 2024
Date Issued:21 January 2025
Review Date:December 2027
Pharmaceutical dosing advice and formulary compliance checked by:Rashmi Selli, Principal Pharmacist for Surgery, January 2025
Key words:Maternal collapse, anaphylaxis, amniotic fluid embolism, toxicity

This guideline has been registered with the trust. However, clinical guidelines are guidelines only. The interpretation and application of clinical guidelines will remain the responsibility of the individual clinician. If in doubt, contact a senior colleague or expert. Caution is advised when using guidelines after the review date.

This guideline is for use in Frimley Health Trust hospitals only. Any use outside this location will not be supported by the Trust and will be at the risk of the individual using it.

Version History

VersionDateGuideline Lead(s)StatusComment
1.0February 2022P. Doncheva, N. RashidFinalFirst cross site version, approved by OCGC, Feb 22
2.0December 2024P Doncheva, S FurnessFinalApproved at Cross Site Obstetric Clinical Governance meeting, 16 December 2024

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